A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220866



Internal ID20787906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141072201..141741000hg38UCSC Ensembl
chr8:142082300..142822361hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38668800
hg19740062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416567
Supporting Variants
Samples
Known GenesDENND3, GPR20, LOC731779, MROH5, PTP4A3, SLC45A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00489


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